Bromocyclopentane
- Product Name
- Bromocyclopentane
- CAS No.
- 137-43-9
- Chemical Name
- Bromocyclopentane
- Synonyms
- CYCLOPENTYL BROMIDE;Bromocylopentane;bromo-cyclopentan;BROMOCYCLOPENTANE;AKOS BBS-00004279;1-Bromocyclopentane;Cyclopentane,bromo-;Bromopentyl bromide;Cyclopentane Bromide;Bromocyclopentane>
- CBNumber
- CB8853084
- Molecular Formula
- C5H9Br
- Formula Weight
- 149.03
- MOL File
- 137-43-9.mol
Bromocyclopentane Property
- Boiling point:
- 137-139 °C (lit.)
- Density
- 1.39 g/mL at 25 °C (lit.)
- refractive index
- n20/D 1.4881(lit.)
- Flash point:
- 95 °F
- storage temp.
- Store at R.T.
- solubility
- Chloroform, Ethyl Acetate (Slightly)
- form
- Liquid
- Specific Gravity
- 1.39
- color
- Clear yellow to light brown
- Water Solubility
- Immiscible with water.
- BRN
- 1209256
- Stability:
- Stable. Flammable. Incompatible with strong oxidizing agents, strong bases.
- InChIKey
- BRTFVKHPEHKBQF-UHFFFAOYSA-N
- LogP
- 2.745 (est)
- CAS DataBase Reference
- 137-43-9(CAS DataBase Reference)
- NIST Chemistry Reference
- Cyclopentane, bromo-(137-43-9)
- EPA Substance Registry System
- Cyclopentane, bromo- (137-43-9)
Safety
- Risk Statements
- 10
- Safety Statements
- 23-24/25-16
- RIDADR
- UN 1993 3/PG 3
- WGK Germany
- 3
- F
- 8
- TSCA
- Yes
- HazardClass
- 3
- PackingGroup
- III
- HS Code
- 29035990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H226Flammable liquid and vapour
- Precautionary statements
-
P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
P233Keep container tightly closed.
P240Ground/bond container and receiving equipment.
P241Use explosion-proof electrical/ventilating/lighting/…/equipment.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P403+P235Store in a well-ventilated place. Keep cool.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- C115207
- Product name
- Bromocyclopentane
- Purity
- ≥98%
- Packaging
- 25g
- Price
- $49.7
- Updated
- 2024/03/01
- Product number
- C115207
- Product name
- Bromocyclopentane
- Purity
- ≥98%
- Packaging
- 100g
- Price
- $55.9
- Updated
- 2024/03/01
- Product number
- B1006
- Product name
- Bromocyclopentane
- Purity
- >98.0%(GC)
- Packaging
- 25g
- Price
- $43
- Updated
- 2024/03/01
- Product number
- B1006
- Product name
- Bromocyclopentane
- Purity
- >98.0%(GC)
- Packaging
- 100g
- Price
- $107
- Updated
- 2024/03/01
- Product number
- A15455
- Product name
- Bromocyclopentane, 98+%
- Packaging
- 100g
- Price
- $44.65
- Updated
- 2024/03/01
Bromocyclopentane Chemical Properties,Usage,Production
Chemical Properties
Bromocyclopentane is a colorless to light yellow liquid at standard temperature and pressure.It has an aroma similar to camphor. It turns brown after a long time. Soluble in ethanol, ether, insoluble in water. Halocyclopentanes can be prepared by reacting the corresponding alcohols with thionyl halides, phosphorus trihalides or hydrohalic acids.
Uses
Bromocyclopentane is a precursor used in the preparation of cyclopentene and cyclopentanol. It is a fatty bromide, which is used as a solvent. It is used as an intermediate for the preparation of surfactant and pharmaceuticals and other organic compounds. It is also used in the production of the medicine cyclopentathiazide.
Preparation
Bromocyclopentane is synthesized by bromination of cyclopentanol: cyclopentanol is mixed with hydrobromic acid and heated to about 170°C refluxed for 6-8h. Then distilled with water steam, the oil layer is washed with 5% sodium carbonate, then dried, filtered, fractionated and collected 136-139°C fraction is the finished product. Another method is by the reaction of cyclopentanol and phosphorus tribromide: the cyclopentanol is cooled to 0 ℃, add the newly evaporated phosphorus tribromide drop by drop, add it all at 0-5 ℃, stir for 2h, and leave it at room temperature overnight. Add water and stratify, take the oil layer water distillation. Distillate stratification, the oil layer was washed with 10% sodium bicarbonate solution, dried with anhydrous calcium chloride, filtration, filtrate distillation, collect 134-141 ℃ fraction that is bromocyclopentane.
Reactions
Bromocyclopentane is reacted with magnesium turnings in dry tetrahydrofuran making cyclopentyl Grignard reagent, a main precursor in the synthesis of Ketamine.
Bromocyclopentane (22.0 g, 0.15 mol) was added to a soln of NaNO2 (18 g, 0.26 mol) in dry DMSO (100 mL) at 15°C and the mixture was stirred at this temperature for 3 h. The mixture was poured into ice water (250 mL) and extracted with petroleum ether (bp 35-37°C; 4 × 50 mL). The combined organic extracts were washed with H2O (4× 50 mL), dried (MgSO4), and concentrated under reduced pressure. The residue was distilled to give Nitrocyclopentane; yield: 9.9 g (58%); bp 62°C/8 Torr; nD/20 1.4538.
Synthesis of Nitrocyclopentane
Synthesis Reference(s)
The Journal of Organic Chemistry, 54, p. 1463, 1989 DOI: 10.1021/jo00267a047
Bromocyclopentane Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from Bromocyclopentane manufacturers
- Product
- Bromocyclopentane 137-43-9
- Price
- US $10.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- 100 mt
- Release date
- 2024-11-27
- Product
- Bromocyclopentane 137-43-9
- Price
- US $9.00/KG
- Min. Order
- 1KG
- Purity
- 99.%
- Supply Ability
- 10 ton
- Release date
- 2024-08-08
- Product
- Bromocyclopentane 137-43-9
- Price
- US $100.00-1.00/KG
- Min. Order
- 1KG
- Purity
- 99%
- Supply Ability
- g-kg-tons, free sample is available
- Release date
- 2023-12-25